|
Index of reports
> Cases with Liver Disorder ()
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Allegra (Fexofenadine) where reactions include liver disorder. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Allegra side effects in 71 year old male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-06-26
Patient: 71 year old male
Reactions: Liver Disorder
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Cefdinir
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-05-28
End date: 2012-06-04
Allegra
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Start date: 2012-05-28
Possible Allegra side effects in 82 year old female
Reported by a pharmacist from Japan on 2012-04-04
Patient: 82 year old female, weighing 52.0 kg (114.4 pounds)
Reactions: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Condition Aggravated, Liver Disorder
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Famotidine
Administration route: Oral
Indication: Drug Eruption
Start date: 2011-07-03
End date: 2011-07-13
Allegra
Administration route: Oral
Indication: Drug Eruption
Start date: 2011-07-06
End date: 2011-07-12
Polaramine
Administration route: Oral
Indication: Drug Eruption
Start date: 2011-07-02
End date: 2011-07-13
Other drugs received by patient: Prednisolone; Heparin Sodium; Cotrim; Corticosteroids; Acetaminophen; Solita-T3 Injection; Lansoprazole; Itraconazole; ALL Other Therapeutic Products; ALL Other Therapeutic Products; Amlodipine Besilate / Candesartan Cilexetil; Plavix
|
